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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818918Generated: November 1, 2026

4-Nitrobenzylamine → HCID 68422863, compound

https://huagongshe.com/reaction/1818918

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzylamineHCID 29147—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantThieno[3,2-d]pyrimidine-4-carboxylic acidHCID 57415848—
SolventDichloromethaneHCID 6344—
ProductHCID 68422863HCID 68422863—

Reaction Steps

To a solution of compound 7.2 (1.0 mmol) and 4-nitrobenzyl amine (1.0 mmol) in dichloromethane (5.0 mL) is added TEA (3.0 equivalents) and O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (“HATU”; 1.1 equivalents). After completion of the reaction, the reaction is partitioned between EtOAc and water. The organic layer is separated, washed with 0.5 N HCl, saturated sodium bicarbonate, brine and dried. Purification by flash column chromatography on silica gel provides thieno[3,2-d]pyrimidine-4-carboxylic acid 4-nitro-benzylamide (compound 7.3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601725B2
Source datasetuspto-grants-2009_10
ORD IDord-df74501d418c410a813a3ad76ba1b264
Source noteuspto-grants-2009_10